FDA Adverse Event
Injury
Summary report: N
QUALA
MDR report key: 211817
·
Received February 26, 1999
Report
- Report Number
- 1412902-1999-00002
- Event Type
- Injury
- Date Received
- February 26, 1999
- Date of Event
- October 28, 1998
- Report Date
- January 22, 1999
- Manufacturer
- MPL TECHNOLOGIES
- Product Code
- DZM
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- KY, US
- Reporter Occupation
- DENTIST
Narratives
Description of Event or Problem · 1
ORAL SURGERY WAS NEEDED TO REMOVE A BROKEN NEEDLE FROM A PT'S GUM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | QUALA | DENTAL NEEDLE | DZM | MPL TECHNOLOGIES | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Required Intervention |